Entry-Level Clinical Research Coordinator – Patient Care Focus

RiseMe; Amarillo (TX); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

401(k) with Company match

Short- and Long-Term Disability

Health Savings Account

Flexible Spending Accounts

Health, Dental and Vision insurance

Generous PTO

Adoption Assistance

Paid Holidays

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator I to support IRB-approved trials, focusing on patient interaction, enrollment, and regulatory compliance. The role requires strong attention to detail and data integrity, with responsibilities across screening, consent, assessments, and data entry.

The candidate will work with investigators, sponsors, and monitors to ensure accurate study execution, efficient site operations, and timely submission of study documentation.

Qualifications

• IRB-approved protocol procedures: identification, screening, randomization, enrollment.
• Direct patient care activities: consenting patients, physical assessments, blood draws, ECG.
• Regulatory compliance, clean data entry, and audit readiness.

Responsibilities

• Take ownership of studies and patients, ensuring protocol adherence.
• Communicate effectively with leadership and team members.
• Maintain regulatory documentation and audit readiness.
• Utilize provided technologies to improve day-to-day efficiency.

Skills

Patient interaction

Attention to detail

Clinical trial coordination

IRB protocol knowledge

Data entry accuracy

Education

Clinical Research Certification (CCRC)

MA certification / medical assistant

Phlebotomy certification

Tools

IRB submission systems

eSource data entry systems

ECG data collection

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator I to support IRB-approved trials, focusing on patient interaction, enrollment, and regulatory compliance. The role requires strong attention to detail and data integrity, with responsibilities across screening, consent, assessments, and data entry.

The candidate will work with investigators, sponsors, and monitors to ensure accurate study execution, efficient site operations, and timely submission of study documentation.